Oxycodone Hydrochloride Tablet
Product Images NDC 63629-1930

4 FDA label images from Bryant Ranch Prepack · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Oxycodone Hydrochloride (NDC 63629-1930). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Fig1

Fig1
A line chart titled 'Oxycodone Dose-Proportionality Study 5 mg, 15 mg and 30 mg (single-dose)' showing concentration (ng/mL) over time (hours). It compares concentration-time profiles for single doses of 5 mg, 15 mg, and 30 mg oxycodone, with curves depicting decreasing concentration from peak values over 25 hours.*
FDA Label Image

Struct

Struct
Chemical structure of oxycodone hydrochloride showing its molecular formula C18H21NO4·HCl and molecular weight 351.82.*
FDA Label Image

Tab2

Tab2
A pharmacokinetic parameters table for oxycodone hydrochloride comparing various doses and formulations, including single-dose tablets (5 mg, 15 mg, 30 mg), oral solutions, and multiple-dose studies. Parameters listed include AUC, Cmax, Tmax, Cmin, Cavg, and half-life, with mean values and standard deviations shown.*
FDA Label Image

Label (Lbl636291930)

Label (Lbl636291930)
Label for Oxycodone Hydrochloride Tablets USP, 30 mg strength, by Bryant Ranch Prepack. The label includes dosage strength, product name, NDC 63629-1930-1, and the manufacturer Ascent Pharmaceuticals, Inc. It indicates a package size of 500 tablets and states Rx only. Storage and cautionary information is also noted.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.